QC Chemist (Entry-Level)

The QC Chemist supports the Quality Control laboratory by performing entry-level analytical testing, sample preparation, documentation, and laboratory support activities in accordance with approved procedures. This role assists with testing of raw materials, in-process materials, finished products, stability samples, and product development samples while developing practical experience in a cGMP-regulated pharmaceutical laboratory. The Junior Chemist is responsible for generating accurate, complete, and contemporaneous laboratory documentation while following all applicable SOPs, safety requirements, and Data Integrity expectations.Key ResponsibilitiesPerform basic and routine analytical testing of raw materials, in-process samples, finished products, stability samples, and product development samples using approved methods and procedures.Prepare samples, standards, reagents, buffers, and mobile phases in accordance with approved procedures and laboratory safety requirements.Support routine laboratory techniques such as wet chemistry, pH testing, titrations, Karl Fischer moisture testing, UV-Vis, FT-IR, dissolution testing, and other basic analytical methods as assigned.Document all testing activities accurately and contemporaneously in laboratory notebooks, worksheets, logbooks, forms, and electronic systems.Verify that instruments, balances, glassware, and equipment are within calibration, qualification, and cleanliness requirements prior to use.Escalate atypical results, documentation issues, equipment concerns, or procedural questions to senior QC personnel or laboratory management.Maintain clean, organized, and inspection-ready laboratory work areas in accordance with cGMP, OSHA, EPA, DEA, and company safety requirements.What We’re Looking ForExperience:0–3 year of laboratory experience required.Academic laboratory experience, internship experience, co-op experience, or prior pharmaceutical laboratory exposure may be considered.Prior experience in a pharmaceutical, cGMP, GLP, analytical, or quality control laboratory preferred but not required.Familiarity with basic laboratory safety, analytical calculations, sample preparation, and documentation practices preferred.Experience with oral solid dosage pharmaceutical testing is a plus but not required.Education:Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a closely related chemistry-based scientific discipline required.Relevant academic laboratory coursework in chemistry, analytical chemistry, pharmaceutical sciences, or instrumental analysis preferred.Skills & Knowledge:Foundational understanding of chemistry, laboratory practices, analytical calculations, and basic sample preparation.Basic familiarity with analytical techniques such as wet chemistry, pH testing, titration, UV-Vis, FT-IR, Karl Fischer, dissolution, and HPLC.Ability to follow approved procedures, test methods, specifications, and written instructions with accuracy and consistency.Strong attention to detail and commitment to accurate, complete, and contemporaneous documentation.Basic understanding of cGMP, GLP, Good Documentation Practices, and Data Integrity expectations preferred.Effective written and verbal communication skills.Proficiency with Microsoft Office applications, including Word and Excel.Familiarity with LIMS, Empower, or other laboratory systems preferred but not required.What We OfferCompetitive compensation with annual performance bonus eligibilityAnnual merit-based pay increasesAutomatic enrollment in a 401(k) at 3% pre-tax with 50% company match on the first 6% contributedPaid Time Off10 paid company holidaysComprehensive medical, dental, vision, and life insurance coverageProfessional development reimbursementCareer growth opportunitiesTuition reimbursement for children and childcare expense reimbursementScheduleFull-time, on-site position (Monday–Friday 8:00 AM - 5:00 PM)